Canonical Allele Identifier: CA2260783748
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43093241_43093242delinsCA , CM000679.2:g.43093241_43093242delinsCA GRCh38
NC_000017.10:g.41245258_41245259delinsCA , CM000679.1:g.41245258_41245259delinsCA GRCh37
NC_000017.9:g.38498784_38498785delinsCA NCBI36
NG_005905.2:g.124742_124743delinsTG , LRG_292:g.124742_124743delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000354071.8:n.2353_2354delinsTG
ENST00000461574.2:c.2289_2290delinsTG ENSP00000417241.2:p.Ser763=
ENST00000470026.6:c.2289_2290delinsTG ENSP00000419274.2:p.Ser763=
ENST00000473961.6:c.2163_2164delinsTG ENSP00000420201.2:p.Ser721=
ENST00000476777.6:c.2286_2287delinsTG ENSP00000417554.2:p.Ser762=
ENST00000477152.6:c.2211_2212delinsTG ENSP00000419988.2:p.Ser737=
ENST00000478531.6:c.784+1502_784+1503delinsTG ENSP00000420412.2:n.784+1502_784+1503delinsTG
ENST00000489037.2:c.2211_2212delinsTG ENSP00000420781.2:p.Ser737=
ENST00000493919.6:c.646+1502_646+1503delinsTG ENSP00000418819.2:n.646+1502_646+1503delinsTG
ENST00000494123.6:c.2289_2290delinsTG ENSP00000419103.2:p.Ser763=
ENST00000497488.2:c.1401_1402delinsTG ENSP00000418986.2:p.Ser467=
ENST00000618469.2:c.2289_2290delinsTG ENSP00000478114.2:p.Ser763=
ENST00000634433.2:c.2166_2167delinsTG ENSP00000489431.2:p.Ser722=
ENST00000644379.2:c.2289_2290delinsTG ENSP00000496570.2:p.Ser763=
ENST00000644555.2:c.646+1502_646+1503delinsTG ENSP00000494614.2:n.646+1502_646+1503delinsTG
ENST00000652672.2:c.2148_2149delinsTG ENSP00000498906.2:p.Ser716=
ENST00000484087.6:c.664+1502_664+1503delinsTG ENSP00000419481.2:n.664+1502_664+1503delinsTG
ENST00000700182.1:c.706+1502_706+1503delinsTG ENSP00000514849.1:n.706+1502_706+1503delinsTG
ENST00000357654.9:c.2289_2290delinsTG MANE Select ENSP00000350283.3:p.Ser763=
ENST00000471181.7:c.2289_2290delinsTG ENSP00000418960.2:p.Ser763=
ENST00000352993.7:c.671-2210_671-2209delinsTG ENSP00000312236.5:n.671-2210_671-2209delinsTG
ENST00000354071.7:c.2289_2290delinsTG ENSP00000326002.7:p.Ser763=
ENST00000357654.7:c.2289_2290delinsTG ENSP00000350283.3:p.Ser763=
ENST00000461221.5:c.*2072_*2073delinsTG ENSP00000418548.1:n.*2072_*2073delinsTG
ENST00000468300.5:c.787+1502_787+1503delinsTG ENSP00000417148.1:n.787+1502_787+1503delinsTG
ENST00000471181.6:c.2289_2290delinsTG ENSP00000418960.2:p.Ser763=
ENST00000478531.5:c.784+1502_784+1503delinsTG ENSP00000420412.1:n.784+1502_784+1503delinsTG
ENST00000484087.5:c.409+1502_409+1503delinsTG ENSP00000419481.1:n.409+1502_409+1503delinsTG
ENST00000487825.5:c.412+1502_412+1503delinsTG ENSP00000418212.1:n.412+1502_412+1503delinsTG
ENST00000491747.6:c.787+1502_787+1503delinsTG ENSP00000420705.2:n.787+1502_787+1503delinsTG
ENST00000493795.5:c.2148_2149delinsTG ENSP00000418775.1:p.Ser716=
ENST00000493919.5:c.646+1502_646+1503delinsTG ENSP00000418819.1:n.646+1502_646+1503delinsTG
ENST00000586385.5:c.5-29291_5-29290delinsTG ENSP00000465818.1:n.5-29291_5-29290delinsTG
ENST00000591534.5:c.-43-18721_-43-18720delinsTG ENSP00000467329.1:n.-43-18721_-43-18720delinsTG
ENST00000591849.5:c.-99+32029_-99+32030delinsTG ENSP00000465347.1:n.-99+32029_-99+32030delinsTG
ENST00000634433.1:c.2166_2167delinsTG ENSP00000489431.1:p.Ser722=
NM_007294.3:c.2289_2290delinsTG , LRG_292t1:c.2289_2290delinsTG NP_009225.1:p.Ser763=
NM_007297.3:c.2148_2149delinsTG NP_009228.2:p.Ser716=
NM_007298.3:c.787+1502_787+1503delinsTG NP_009229.2:n.787+1502_787+1503delinsTG
NM_007299.3:c.787+1502_787+1503delinsTG NP_009230.2:n.787+1502_787+1503delinsTG
NM_007300.3:c.2289_2290delinsTG NP_009231.2:p.Ser763=
NR_027676.1:n.2425_2426delinsTG
NM_007294.4:c.2289_2290delinsTG MANE Select NP_009225.1:p.Ser763=
NM_007297.4:c.2148_2149delinsTG NP_009228.2:p.Ser716=
NM_007299.4:c.787+1502_787+1503delinsTG NP_009230.2:n.787+1502_787+1503delinsTG
NM_007300.4:c.2289_2290delinsTG NP_009231.2:p.Ser763=
NR_027676.2:n.2466_2467delinsTG